Canonical Allele Identifier: CA983867509
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs2056042140
gnomAD v3: 17-42903863-T-C
gnomAD v4: 17-42903863-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42903863T>C , CM000679.2:g.42903863T>C GRCh38
NC_000017.10:g.41055880T>C , CM000679.1:g.41055880T>C GRCh37
NC_000017.9:g.38309406T>C NCBI36
NG_011808.1:g.8066T>C , LRG_147:g.8066T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.231-68T>C MANE Select ENSP00000253801.1:n.231-68T>C
ENST00000253801.6:c.231-68T>C ENSP00000253801.1:n.231-68T>C
ENST00000585489.1:c.231-68T>C ENSP00000466202.1:n.231-68T>C
ENST00000588481.1:n.296-68T>C
ENST00000592383.5:c.231-68T>C ENSP00000465958.1:n.231-68T>C
NM_000151.3:c.231-68T>C NP_000142.2:n.231-68T>C
NM_001270397.1:c.231-68T>C NP_001257326.1:n.231-68T>C
NM_000151.4:c.231-68T>C MANE Select NP_000142.2:n.231-68T>C
NM_001270397.2:c.231-68T>C NP_001257326.1:n.231-68T>C
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